Canonical Allele Identifier: CA379664601
Gene: CTR9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.10785260C>G (hg19) chr11:g.10763713C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.10763713C>G , CM000673.2:g.10763713C>G GRCh38
NC_000011.9:g.10785260C>G , CM000673.1:g.10785260C>G GRCh37
NC_000011.8:g.10741836C>G NCBI36
NG_051671.1:g.17727C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000361367.7:c.1028C>G MANE Select ENSP00000355013.2:p.Pro343Arg
ENST00000361367.6:c.1028C>G ENSP00000355013.2:p.Pro343Arg
ENST00000524523.1:c.881C>G ENSP00000431458.1:p.Pro294Arg
NM_014633.4:c.1028C>G NP_055448.1:p.Pro343Arg
NM_001346279.1:c.1028C>G NP_001333208.1:p.Pro343Arg
NM_014633.5:c.1028C>G MANE Select NP_055448.1:p.Pro343Arg
NM_001346279.2:c.1028C>G NP_001333208.1:p.Pro343Arg
Search 100 bp 5'
Search 100 bp 3'